Definition

The representation of a medicinal product as it is supplied in a package that contains within the package more than one type of clinical drug. 

Use Cases

The use cases supported by the Combination (Real) Packaged Clinical Drug concept type are the same as those for the basic real packaged clinical drug, with the additional detail that administration records may wish to identify which of the particular component clinical drugs were administered at any particular point in time administration event (using AIDC or similar).

Discussion

For abstract concepts, the combination packaged clinical drug, contains two or more different clinical drugs.

For real concepts, the combination real packaged clinical drug contains two or more different real clinical drugs.  The package is placed in the supply chain using a single name (which may be a trade or brand name) by a single supplier organisation, even if one or more of the component real clinical drugs is sourced from a different organisation; for this reason, the 774158006 |Has product name| and 774159003 |Has supplier| attributes are optionally included.

A combination packaged clinical drug may also be called a "component product" or a "multi-component package" as the product itself is a package that contains more than one type of component element (clinical drug) within it; it may also be known as or a "kit" or a "combination medicinal product". Occasionally a combination packaged clinical drug is may be known as a "compound product" but this term risks being confused with products that are extemporaneously compounded by a pharmacist from a formula provided by the prescriber for an individual patient (sometimes also known as "magistral products").

Examples of combination packaged clinical drug include:

• A package containing clotrimazole cutaneous cream and one or more clotrimazole vaginal tablets for treatment of vaginal candidiasis
• A package containing clotrimazole cutaneous cream and one or more fluconazole oral capsules for treatment of vaginal candidiasis
• A package containing combinations of ethinylestradiol and levonorgestrel tablets in different strengths and which may also include inert tablets for oral contraception (note that in this example, the components are themselves multi-ingredient items)
• A package containing amoxicillin, clarithromycin and lansoprazole for treatment of Helicobacter infection
• A package containing a budesonide dispersible tablet and the vehicle to disperse it in, to make a rectal solution for treatment of colitis
• A package containing rasburicase 1.5 mg powder for solution for injection and the diluent solution

This specification for national drug extensions recommends that a combination packaged clinical drug should be represented only as packaged products (real packaged clinical drugs and, if an abstract representation is required, as packaged clinical drugs), with their individual components represented as clinical drugs. For practical implementation of a national terminology, mechanisms such as reference sets may be used to include combination packaged clinical drug with other classes of medicinal product (such as clinical drugs) to aid users in finding and selecting these products. 

The following diagram gives an example of how the packaged medicinal product classes should be used to describe combination medicinal products:

Figure 39: Diagram of options for a national extension describing combination real packaged clinical drugs

In some representations of combination packages, and particularly in ISO 11615 in IDMP, a "combined dose form" concept is used in the name of the combination product (for example "pessary and cream"). Although useful as a concept to describe the dose form using a single attribute and value, a combination dose form concept does not easily support knowing which component has which dose form. The model used here, whereby each clinical drug is described with its appropriate dose form and they are brought together into the packaged product containing the components does not require the use of combination dose form concepts. 

For those combination packages that contain a diluent as an item in the package, national extensions may decide not to explicitly describe the diluent as a component, but merely to describe its presence in the text of the fully specified name for the real packaged medicinal product; alternatively the national extension may author a "diluent" clinical drug concept and use that as one of the components of the combination product. If the constitution of the diluent is known (e.g. water for injections, 0.9% sodium chloride solution for injection), the clinical drug for the diluent can be explicitly described.  Dual chamber products containing the two components (where one is the diluent) in a single unit of presentation can be described as combination products if required.

Attributes

The following table describes the attributes for combination (real) packaged clinical drugs in a national extension.

The (real) packaged clinical drug class is related to the clinical drug class by a composition relationship relationship, and therefore the attribute "contains clinical drug" is used to make the association between the packaged clinical drug and the clinical drugs it contains. 

Representation of packaged medicinal products should use Clinical Drugs that have presentation strength (either only or in addition to concentration strength) whenever possible in order to be able to accurately describe the number of presentation units present in the package. The exception will be for continuous products such as semi-solid dose forms of creams, gels etc. where strength pattern 3a is used (see international Editorial Guidelines). In all cases the pack size and pack size unit should relate to the denominator unit of the strength.

Example Diagrams

Example: combination packaged clinical drug: stated view followed by the inferred view

Figure 40: Example of a combination packaged clinical drug - stated view

Figure 41: Example of a combination packaged clinical drug - inferred view

Example: combination real packaged clinical drug: stated view followed by the inferred view

Figure 42: Example of a combination real packaged clinical drug - stated view

Figure 43: Example of a combination real packaged clinical drug - inferred view

IDMP Compatibility

Since the ISO 11615 standard treats all Packaged Medicinal Products in the same manner, whether they are standard products or combination products, because the associations between the manufactured item(s) present in the package are described using recursive relationships, the Combination Real Packaged Medicinal Product is equivalent to a Packaged Medicinal Product identified by a PCID. As with the Real Packaged Medicinal Product. the Combination Real Packaged Medicinal Product  is a representation of the "real world product" authorised for sale and/or supply that exists for all jurisdictions and which is marketed into the supply chain for use, it is a concept that should form the 1:1 join between representation in the regulatory domain (IDMP) and representation in the clinical domain (SNOMED CT and national medicinal product terminologies), even if some national medicinal product terminologies choose not to represent it.